Polymer Chemistry Author of the Week- Steve Howdle

Steve Howdle is currently leading his research group in the School of Chemistry, The University of Nottingham, UK. His main research interests are supercritical fluids, biomaterials, polymer modification, polymer composites, nanocomposites and devices. Steve is the chairman of the Macro Group UK, which is a joint interest group of the Royal Society of Chemistry and Society of Chemical Industry. Steve is also coach of the Toton Tigers Under 10s football squad and holds an official coaching award of the English FA.

Please follow the link to get more information about Steve’s research group and his recent paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?

Just like many others, I was inspired by some very good chemistry teachers when I was at School – flashes, bangs, flames and smells – all the things that still attract young people to chemistry!

What was the motivation behind the research in your recent Polymer Chemistry paper?

I’ve been working with supercritical carbon dioxide for most of my career.  The world  has a problem with CO2 – and a great deal of effort and money is being channelled into collecting and storing it. I think we really ought to be using it!  Some chemists are activating it, some are polymerising it, I think that if just some of that CO2 could replace other solvents this could have a  large impact which would be very positive for the environment.  But it’s more than that – we have shown that there are many cases where you can carry out a reaction or a process in supercritical CO2 that you simply cannot achieve in a normal solvent – so there could be very real advantages to using CO2 – and that has been a major driver for my research recently with applications from polymer and material synthesis through to tissue engineering and drug delivery.

This particular paper is focussed on showing that some new inexpensive  polymers have high solubility in CO2 and could be used as effective surfactants and stabilisers for CO2. Up till now, only fluorinated and silicone based materials showed significant solubility, and these can be expensive and are not always environmentally benign. We hope that our paper will show that alternative, cheaper materials could be used, and hence open up more opportunities to exploit supercritical carbon dioxide.

Why did you choose Polymer Chemistry to publish your work?

It’s the first RSC Journal focussed on Polymers, and it really is a natural choice for quite a lot of my research.  This is my first paper in PC – but I’m sure there will be more!

In which upcoming conferences may our readers meet you?

The next conference I will be going to is quite unusual – The 6th Scientific and Engineering Conference with International Participation “Supercritical Fluids: Fundamentals, Technologies, Innovations” is being held on the shores of Lake Baikal, Siberia in early July!

How do you spend your spare time?

I have two teenage boys – both competitive swimmers – and I spend a lot of my time ferrying them to training and competitions (I’m writing these answers by the pool!).  I also love football, I still play (for a Veterans’ team) and I also coach kids – I am the manager of the Toton Tigers U13s squad.

Which profession would you choose if you were not a scientist?
Football player– but I wasn’t good enough!

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Photodecarbonylation and photoinitiated polymerization from a monomer and polymer based on the α-keto ester methacryloyl phenylglyoxylate

Researchers from Clarkson University have synthesised an α-keto ester methacryloylethyl phenylglyoxylate (MEPG), and its homopolymer, and tested their photoinitiation capabilities in a crosslinking monomer resin system.

This resin system contained bis-phenol A-glycidyl methacrylate (BisGMA) and triethylene glycol dimethacrylate (TEGDMA). The CO evolution from the photoinduced decarbonylation led to a significant reduction in the volume shrinkage of the resin upon photocuring with UV light. The addition of an inorganic filler (SiO2) to the resin did not affect the CO generation and further reduced the volume shrinkage.

Interested to know more? Why not read the full article for free: K. Omrane, J.-J. Feng, R. E. Partch and D. A. Shipp, Polym. Chem., 2011, 2, 1307–1311.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Overcoming the PEG-addiction: well-defined alternatives to PEG, from structure–property relationships to better defined therapeutics

Poly(ethylene glycol) is one of the most frequently used polymers for biomedical applications.

In this review, recent developments in controlled polymerisation techniques – and particularly those they allow alternatives to PEG – are highlighted. Key to the biological application of these techniques is a method by which to improve the properties of polymer therapeutics and several are presented in this review. However, a more comprehensive understanding of the complex interactions of synthetic materials with the numerous biological entities and barriers in the human body is necessary in order fine-tune their therapeutic impact.

Interested to know more? Why not read the full article for free: M. Barz, R. Luxenhofer, R. Zentel and M. J. Vicent, Polym. Chem., 2011, DOI: 10.1039/c0py00406e (Advance Article)

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week – Heather Maynard

Heather D. Maynard received a B.S. with Honors in Chemistry from the University of North Carolina at Chapel Hill and a M.S. in Materials Science from the University of California, Santa Barbara. Her Ph.D. from the California Institute of Technology was awarded in the summer of 2000 for research in the group of Nobel Prize winner Robert Grubbs. She then moved to the laboratory of Jeffrey Hubbell at the Swiss Federal Institute of Technology in Zurich (ETH), where from 2000-2002 she was an American Cancer Society Postdoctoral Fellow. Dr. Maynard joined the UCLA faculty as an Assistant Professor in August 2002 as the first Howard Reiss Career Development Chair in the Department of Chemistry and Biochemistry and as a member of the California NanoSystems Institute.  She is now an Associate Professor.  Maynard’s research interests include polymer synthesis, biohybrid materials, surface modification, and nanomedicine.

Please follow the link to get more information about Heather’s group and her recent paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?
I have always been curious about how things work and like solving puzzles. In junior high I took a science class with a terrific teacher that covered physics, chemistry, and biology.  Although I enjoyed all of them, it was chemistry that really sparked my interest.  Even then the idea that I could come to understand the world around me at a molecular level and could create new materials enthralled me. At the age of twelve I decided to be a chemistry professor.

What was the motivation behind the research in your recent Polymer Chemistry paper? (DOI: 10.1039/C1PY00034A)
One of my main research interests is the synthesis and application of protein-polymer conjugates.  These conjugates are utilized as therapeutics to treat a range of human diseases, so we considered the synthesis and mode of action of known protein therapeutics.  The paper summarizes all of the FDA approved protein-polymer conjugates.  We teamed up with a medical doctor at UCLA to write this review, which describes the synthesis of these materials, as well as the biological activity, administration, and where possible the half-life information.  Since there are many polymer chemists interested in bioconjugates, we anticipated that a concise review of currently used therapeutics would be useful to the community.

Why did you choose Polymer Chemistry to publish your work?
Polymer Chemistry is an exciting new journal by the RSC, and we were pleased to be invited to take part in a themed issue on Polymer Bioconjugates.

In which upcoming conferences may our readers meet you?
I will attend the International Conference on Materials for Advanced Technologies in Singapore in June and the American Chemical Society Fall National Meeting in Denver.

How do you spend your spare time?
I enjoy spending time with my family and also like to mountain bike.

Which profession would you choose if you were not a scientist?
That is a hard question to answer as it is very difficult to imagine myself not a scientist.  Perhaps I would enjoy being an astronaut.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry issue 6 out now!

On the front cover of issue 6 is An optical-logic system based on cationic conjugated polymer/DNA/intercalating dyes assembly for label-free detection of conformational conversion of DNA i-motif structure by Wei Huang and co-workers at Nanjing University of Posts & Telecommunications. The paper describes a strategy for the design, construction, and characterization of a novel supramolecular optical-logic system based on the assembly of a cationic conjugated polymer, DNA, and intercalating dyes.

The issue also contains three Hot Articles.

Read the full issue here:

Follow Polymer Chemistry on Twitter

 Polymer Chemistry News on Facebook

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Covalently incorporated protein–nanogels using AGET ATRP in an inverse miniemulsion

Covalently linked protein–nanogel hybrids (PNHs) have been synthesized using AGET ATRP in an inverse miniemulsion.

A genetically engineered protein, which contained a non-natural amino acid bearing an ATRP initiator, has been used to synthesise protein–nanogel hybrids by electron transfer ATRP in an inverse miniemulsion. This is an appropriate synthetic strategy to covalently, site specifically incorporate green fluorescent proteins into well-defined nanogels. The hybrids are expected to be suitable for potential controlled release applications.

Interested to know more? Why not read the full article for free: S. E. Averick, A. J. D. Magenau, A. Simakova, B. F. Woodman, A. Seong, R. A. Mehl and K. Matyjaszewski, Polym. Chem., 2011, DOI: 10.1039/c1py00050k (Advance Article)

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Photo-responsive, biocompatible polymeric micelles self-assembled from hyperbranched polyphosphate-based polymers

Researchers from Zhejiang University have constructed photo-responsive, biocompatible micelles from amphiphilic diazonaphthoquinone-modified hyperbranched polyphosphates.

HPHEEP–DNQ was synthesised by modification of hydrophilic hyperbranched polyphosphate (HPHEEP) with hydrophobic, light-responsive 2-diazo-1,2-naphthoquinone (DNQ). This polymer could then self-assemble into micelles. Model drug coumarin 102 was encapsulated into these micelles and its controlled release by UV irradiation was confirmed by fluorescence spectroscopy. It was also proved that the micelles had excellent biocompatibility.

Interested to know more? Why not read the full article for free: C. Chen, G. Liu, X. Liu, S. Pang, C. Zhu, L. Lv and J. Ji, Polym. Chem., 2011, DOI: 10.1039/C1PY00094B (Advance Article)

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week-Brent Sumerlin


Brent Sumerlin is Harold Jeskey Trustee Associate Professor in Department of Chemistry at Southern Methodist University. His research group focuses on well-defined polymeric materials with selected functionality, composition, and molecular architecture.  Their particular interest is on polymers that are water-soluble and stimuli-responsive. Such “smart” polymers have the ability to self-assemble or dissociate in solution in response to changes in their surroundings. Potential target applications include controlled and targeted drug delivery, surface modification, and the synthesis of self-healing materials. Their further interests are at the interface of bio-, organic, and polymer chemistry, with particular focus on fusing the fields to prepare materials with synergistic properties. Please follow the link for further information on Brent’s research group and his recent paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?
One of my high school chemistry instructors, Mr. Philip R. Dail, taught with such infectious enthusiasm that it became impossible for me to imagine becoming anything other than a chemist.

What was the motivation behind the research in your recent Polymer Chemistry paper?
For the last few years, we have attempted to capitalize on our expertise in the area of water-soluble polymers and controlled polymer synthesis to modify proteins with polymers for potential therapeutic and catalytic applications. Exciting work by several groups has shown that controlled radical polymerization (CRP) is ideal for the preparation of polymer-protein conjugates. In our opinion, one of the most significant qualities of CRP is that it enables the preparation of block copolymers by the sequential polymerization of two monomers. Therefore, we thought it was important to demonstrate the potential of CRP for the direct synthesis of block copolymer-protein conjugates.

Why did you choose Polymer Chemistry to publish your work?
We approach the synthesis of polymer-protein conjugates from the perspective of polymer chemists rather than biochemists. One basic method to demonstrate control during a “living” polymerization process is to investigate the retention of end group functionality by chain extension during a second polymerization. Indeed, we thought any polymerization we conducted by grafting from a protein should be judged by the same criteria that would be applied to controlled polymerizations with more traditional low molecular weight initiators (or chain transfer agents, in the case of RAFT). Therefore, we think these findings are exciting and fundamental polymer chemistry results and that Polymer Chemistry is the ideal venue in which to highlight them.

In which upcoming conferences may our readers meet you?
I will attend the Polymers Gordon Research Conference at Mount Holyoke College in Massachusetts in June 2011 and the National Meeting of the American Chemical Society in Denver, Colorado in August 2011. The results from our recent paper will be presented in Denver in the International Year of Chemistry Symposium: Controlled Radical Polymerization that I am co-organizing with Professors Krzysztof Matyjaszewski (Carnegie Mellon University) and Nicolay Tsarevsky (Southern Methodist University).

How do you spend your spare time?
Generally, I’m happily chauffeuring my two daughters to school, ballet, gymnastics, and birthday parties. If I have time on my own, I enjoy reading.

Which profession would you choose if you were not a scientist?
I think I would also have enjoyed journalism. I would love the opportunity to travel and cover current events – especially if I were allowed to editorialize!

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Architecture effects on L-selectin shedding induced by polypeptide-based multivalent ligands

Architecture effects on L-selectin shedding induced by polypeptide-based multivalent ligands: Polymers can be used as multivalent backbones to probe cell surface receptor arrangement and cell signalling. In this hot paper Shuang Liu and Kristi Kiick synthesize a series of polypeptide-based multivalent ligands and study the architecture effects on L-selectin shedding using by L-selectin shedding assay and ELISA. The team claim that these polypeptide-based multivalent ligands may have potential physiological and pathological applications as cell biology tools, and in the regulation of cell functions or inflammatory responses. (Polym. Chem., 2011, DOI: 10.1039/C1PY00063B, Advance Article)

Graphical abstract: Architecture effects on L-selectin shedding induced by polypeptide-based multivalent ligands

Interested to know more? Why not read the full article available for free until 6th June.

Polymer Chemistry News on TwitterFind Polymer Chemistry on Facebook

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week – Bert Klumperman


Bert Klumperman is a professor in the Department of Chemistry and Polymer Science in University of Stellenbosch, South Africa. Bert is very well known in the Polymer Science field with his studies on understanding the kinetics of radical polymerization reactions. Their research is based on not only mechanistic and kinetic studies but also the synthesis of advanced macromolecular structures for various applications. Please follow the links for further information on Bert’s research group and his current paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?
During secondary school I was very much attracted to science topics (mainly mathematics, biology and chemistry). After initial thoughts on studying biology, I decided to go for chemistry and chemical engineering at Twente University (Netherlands). In my current position in Stellenbosch (South Africa) I get many opportunities to collaborate with scientists in Biochemistry, Microbiology, Pharmacology and the Medical School. I greatly enjoy this direction of my research.

What was the motivation behind the research in your recent Polymer Chemistry paper? (DOI: 10.1039/c1py00069a)
Throughout my career (initial industrial career at DSM Research, later academic career at Eindhoven University of Technology and Stellenbosch University), poly(styrene-co-maleic anhydride) (SMA) has always played a big role. It is almost like a red line through my entire career up to this point. In 2009, my colleague Prof Peter Mallon and I supervised a student who worked for a number of weeks on electrospinning of SMA. She showed that there are very interesting possibilities in terms of post-spinning modification. Among the many experiments she tried to immobilize a protein (lysozyme), which seemed to work. In 2010, we continued this work with an Honours student (William Cloete), who immobilized the enzymes described in the paper. In collaboration with a student from Biochemistry (Craig Adriaanse) from the group of Prof Pieter Swart, he carried out the enzyme immobilization and the characterization in terms of enzyme activity. It turned out that such a facile immobilization technique on a solid, high surface area membrane works very well.

Why did you choose Polymer Chemistry to publish your work?
I already had very positive experience with Polymer Chemistry for the publication of an earlier paper. The layout is done very nicely and, in general, they publish high quality work. It will be very interesting to see what their first Impact Factor (IF) is going to be. I would not be surprised if they manage to compete with the very top journals in the field of Polymer Science in terms of IF. For me at least, Polymer Chemistry will remain a serious candidate for publishing my future work.

In which upcoming conferences may our readers meet you?
After a conference in Turkey (Antalya, LRP’11) in mid-April, and one in my home town Stellenbosch (UNESCO/IUPAC Conference on Macromolecules and Materials) at the end of April, the next one will again be in South Africa. From 22-26 May, I will be in Pretoria to attend the 11th International Conference on Frontiers of Polymers and Advanced Materials. After that it will be quiet for a while and I will only attend the ACS National Meeting in Denver (28 August – 1 September), where Prof Kris Matyjaszewski will co-organize the 6th edition of an international symposium on Controlled/Living Radical Polymerization.

How do you spend your spare time?
Ever since I was 10 years old, I have actively played musical instruments. Initially I played the clarinet in a wind orchestra and several smaller bands. When I worked full-time in Eindhoven, I played clarinet in one of the top amateur wind orchestras of the Netherlands (“Koninklijke Harmonie Oefening & Uitspanning” from Beek en Donk) with which I participated in the World Music Contest in Kerkrade (Netherlands) in 1997. Just over 10 years ago, I switched to play the oboe. After a few years of practicing, I started to play the 1st oboe in a small symphony orchestra in Wassenaar (Netherlands), which I did for three years. At that time I had taken up my current position at Stellenbosch University (South Africa), which made it impossible to continue. Currently, I am still taking oboe lessons and at this very moment practicing Mozarts Oboe Quartet in F-major, which I hope to play with a violin, viola and cello in the second half of the year at some informal occasion in Stellenbosch.

Which profession would you choose if you were not a scientist?
This is the most difficult question to answer. The most obvious answer would be a professional musician, which in actual fact I have considered at some point. However, also several professions in the medical world would be serious candidates.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)